EP0707344B1 - Halbleiteranordnung mit einer dünnen Polysilicium-Schicht und Verfahren zur Herstellung - Google Patents

Halbleiteranordnung mit einer dünnen Polysilicium-Schicht und Verfahren zur Herstellung Download PDF

Info

Publication number
EP0707344B1
EP0707344B1 EP95114554A EP95114554A EP0707344B1 EP 0707344 B1 EP0707344 B1 EP 0707344B1 EP 95114554 A EP95114554 A EP 95114554A EP 95114554 A EP95114554 A EP 95114554A EP 0707344 B1 EP0707344 B1 EP 0707344B1
Authority
EP
European Patent Office
Prior art keywords
thin film
film
gas
crystal
silicon
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP95114554A
Other languages
English (en)
French (fr)
Other versions
EP0707344A3 (de
EP0707344A2 (de
Inventor
Hideo Miura
Shunji Moribe
Hisayuki Kato
Atsuyoshi Koike
Shuji Ikeda
Asao Nishimura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Ltd
Original Assignee
Hitachi Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Ltd filed Critical Hitachi Ltd
Priority to EP02001183A priority Critical patent/EP1209726A3/de
Publication of EP0707344A2 publication Critical patent/EP0707344A2/de
Publication of EP0707344A3 publication Critical patent/EP0707344A3/de
Application granted granted Critical
Publication of EP0707344B1 publication Critical patent/EP0707344B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/24Deposition of silicon only
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/38Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by treatments done after the formation of the materials
    • H10P14/3802Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45512Premixing before introduction in the reaction chamber
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45523Pulsed gas flow or change of composition over time
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/455Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45561Gas plumbing upstream of the reaction chamber
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/52Controlling or regulating the coating process
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00Field-effect transistors [FET]
    • H10D30/01Manufacture or treatment
    • H10D30/021Manufacture or treatment of FETs having insulated gates [IGFET]
    • H10D30/031Manufacture or treatment of FETs having insulated gates [IGFET] of thin-film transistors [TFT]
    • H10D30/0312Manufacture or treatment of FETs having insulated gates [IGFET] of thin-film transistors [TFT] characterised by the gate electrodes
    • H10D30/0314Manufacture or treatment of FETs having insulated gates [IGFET] of thin-film transistors [TFT] characterised by the gate electrodes of lateral top-gate TFTs comprising only a single gate
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00Field-effect transistors [FET]
    • H10D30/01Manufacture or treatment
    • H10D30/021Manufacture or treatment of FETs having insulated gates [IGFET]
    • H10D30/031Manufacture or treatment of FETs having insulated gates [IGFET] of thin-film transistors [TFT]
    • H10D30/0321Manufacture or treatment of FETs having insulated gates [IGFET] of thin-film transistors [TFT] comprising silicon, e.g. amorphous silicon or polysilicon
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D62/00Semiconductor bodies, or regions thereof, of devices having potential barriers
    • H10D62/40Crystalline structures
    • H10D62/405Orientations of crystalline planes
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D64/00Electrodes of devices having potential barriers
    • H10D64/01Manufacture or treatment
    • H10D64/011Manufacture or treatment of electrodes ohmically coupled to a semiconductor
    • H10D64/0111Manufacture or treatment of electrodes ohmically coupled to a semiconductor to Group IV semiconductors
    • H10D64/0113Manufacture or treatment of electrodes ohmically coupled to a semiconductor to Group IV semiconductors the conductive layers comprising highly doped semiconductor materials, e.g. polysilicon layers or amorphous silicon layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D64/00Electrodes of devices having potential barriers
    • H10D64/01Manufacture or treatment
    • H10D64/013Manufacture or treatment of electrodes having a conductor capacitively coupled to a semiconductor by an insulator
    • H10D64/01302Manufacture or treatment of electrodes having a conductor capacitively coupled to a semiconductor by an insulator the insulator being formed after the semiconductor body, the semiconductor being silicon
    • H10D64/01304Manufacture or treatment of electrodes having a conductor capacitively coupled to a semiconductor by an insulator the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor
    • H10D64/01306Manufacture or treatment of electrodes having a conductor capacitively coupled to a semiconductor by an insulator the insulator being formed after the semiconductor body, the semiconductor being silicon characterised by the conductor the conductor comprising a layer of silicon contacting the insulator, e.g. polysilicon
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10DINORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D64/00Electrodes of devices having potential barriers
    • H10D64/60Electrodes characterised by their materials
    • H10D64/66Electrodes having a conductor capacitively coupled to a semiconductor by an insulator, e.g. MIS electrodes
    • H10D64/661Electrodes having a conductor capacitively coupled to a semiconductor by an insulator, e.g. MIS electrodes the conductor comprising a layer of silicon contacting the insulator, e.g. polysilicon having vertical doping variation
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10FINORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
    • H10F71/00Manufacture or treatment of devices covered by this subclass
    • H10F71/121The active layers comprising only Group IV materials
    • H10F71/1221The active layers comprising only Group IV materials comprising polycrystalline silicon
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/24Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials using chemical vapour deposition [CVD]
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/29Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by the substrates
    • H10P14/2901Materials
    • H10P14/2902Materials being Group IVA materials
    • H10P14/2905Silicon, silicon germanium or germanium
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/32Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by intermediate layers between substrates and deposited layers
    • H10P14/3202Materials thereof
    • H10P14/3238Materials thereof being insulating materials
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/34Deposited materials, e.g. layers
    • H10P14/3402Deposited materials, e.g. layers characterised by the chemical composition
    • H10P14/3404Deposited materials, e.g. layers characterised by the chemical composition being Group IVA materials
    • H10P14/3411Silicon, silicon germanium or germanium
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/34Deposited materials, e.g. layers
    • H10P14/3438Doping during depositing
    • H10P14/3441Conductivity type
    • H10P14/3442N-type
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/34Deposited materials, e.g. layers
    • H10P14/3466Crystal orientation
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/40Formation of materials, e.g. in the shape of layers or pillars of conductive or resistive materials
    • H10P14/42Formation of materials, e.g. in the shape of layers or pillars of conductive or resistive materials using a gas or vapour
    • H10P14/43Chemical deposition, e.g. chemical vapour deposition [CVD]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/546Polycrystalline silicon PV cells
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Definitions

  • This invention relates to method for producing a thin film electrode of a semiconductor device prevented from changes of internal stress in a silicon thin film and generation of crystal defects caused by the changes of internal stress.
  • a silicon thin film is used as electrodes and/or a wiring material. Since the silicon thin film is a semiconductor material, it is necessary to reduce electric resistance when used as a wiring material. In general, it is doped with an element of group III or V (e.g. B, P, As, etc.) by diffusion. In the doping with such an impurity, there has been employed thermal diffusion from film surface or ion implantation.
  • group III or V e.g. B, P, As, etc.
  • JP-A-03 070 126 describes a method for production of an electrode having a low electric resistance by forming a silicon dioxide film and a gate oxide film on a p-type silicon substrate, adding an impurity to a channel section, depositing an amorphous silicon film for a gate electrode by a CVD method, heat treating at 600°C or higher to carry out polycrystallisation, adding n-type impurity and activation of the impurity by subsequent heat treatment.
  • a polycrystalline silicon thin film is formed the crystal grains of which are oriented with their [111] axes in the vertical direction of the substrate surface.
  • US 5,318,919 describes a manufacturing method of a thin film transistor using an in-situ doping technique.
  • a pure amorphous silicon layer having a thickness of approximately 1 ⁇ m and an in-situ doped n-type conductive amorphous silicon layer are laminated on a glass substrate.
  • the laminated layers are annealed at temperatures below 600° to result in a polycrystalline silicon film.
  • a part of the surface of the polycrystalline silicon film is removed by etching where the gate electrode is to be formed, followed by formation of an insulative film. Thereafter, a metallic gate electrode is formed on the insulative film.
  • the polycrystalline silicon thin film can be formed at low temperatures using a cheap glass substrate without implantation of a dopant.
  • DE 41 38 057 Al describes a semiconducor device having a polycrystalline silicon layer as a gate electrode the crystal grains of which are oriented in a particular direction what is achieved by the conventional LPCVD method including the control of the deposition temperature in the range of 550 to 620°C.
  • GB 2 254 960 A describes a conventional LPCVD process which is used to deposit an amorphous silicon layer at temperatures of 510 to 560°C and an overlying polycrystalline silicon layer at a higher temperature of 610 to 640°C on a gate oxide layer of a substrate.
  • the layer structure is converted into polycrystalline silicon by annealing.
  • the resulting upper polysilicon layer has a larger grain size as compared to the lower polysilicon layer and the diffusion of P- ions which are incorporated by the thermal diffusion is minimised.
  • the method of the invention provides a semiconductor device comprising a semiconductor substrate, an underlying film formed thereon and a silicon thin film doped with an impurity selected from group III and V elements and formed on the underlying film, crystal grains of said silicon thin film having mainly a columnar structure grown from an interface of the underlying film to a surface of the silicon thin film, and a crystal orientation on film surfaces of at least 60% of the individual crystal grains being in an uniform direction.
  • the present invention also provides a process for producing a semiconductor device, which comprises forming an underlying film on a semiconductor substrate, and forming a silicon thin film on the underlying film by depositing a silicon film having no impurity from a SiH 4 gas or a Si 2 H 6 gas to a thickness of 1 nm or more, followed by deposition of the silicon film doped with an impurity selected from group III and V elements.
  • a silicon film having no impurity from a SiH 4 gas or a Si 2 H 6 gas to a thickness of 1 nm or more
  • an impurity selected from group III and V elements When an amorphous silicon thin film is deposited, heat treatment is conducted to finally provide a polycrystalline silicon thin film.
  • the present invention still further provides a process for producing a silicon thin film, which comprises introducing into a reaction chamber a raw material gas selected from SiH 4 gas and Si 2 H 6 gas to deposit a silicon film having no impurity to a thickness of 1 to 10 nm, followed by introduction of an impurity gas selected from group III and V elements together with the raw material gas to deposit a silicon film doped with the impurity.
  • a process for producing a silicon thin film which comprises introducing into a reaction chamber a raw material gas selected from SiH 4 gas and Si 2 H 6 gas to deposit a silicon film having no impurity to a thickness of 1 to 10 nm, followed by introduction of an impurity gas selected from group III and V elements together with the raw material gas to deposit a silicon film doped with the impurity.
  • an impurity gas selected from group III and V elements together with the raw material gas to deposit a silicon film doped with the impurity.
  • Fig. 1 is a cross-sectional view of one example of the semiconductor device immediately after the film deposition according to the present invention.
  • Fig. 2 is a cross-sectional view of the same example of the semiconductor device after heat treatment according to the present invention.
  • Fig. 3 is an electron microscope photograph showing the structure of growing crystal at a cross-section of P-doped amorphous silicon thin film.
  • Fig. 4 is an electron microscope photograph showing the structure of growing crystal at a plane of P-doped amorphous silicon thin film.
  • Fig. 5 is an electron microscope photograph showing the structure of growing crystal at a cross-section of P-doped amorphous silicon thin film when the non-doped layer is formed.
  • Fig. 6 is an electron microscope photograph showing the structure of growing crystal at a plate of P-doped amorphous silicon thin film when the non-doped layer is formed.
  • Fig. 7 is a flow chart explaining one example of the process for depositing the thin film.
  • Fig. 8 is a cross-sectional view of a further example of the semiconductor device immediately after the film deposition according to the present invention.
  • Fig. 9 is a cross-sectional view of a transistor according to the present invention.
  • Fig. 10 is a cross-sectional view of a gate electrode according to the present invention.
  • Fig. 11 is a cross-sectional view of a flash memory according to the present invention.
  • Fig. 12 is a schematic view of a chemical vapor deposition apparatus according to the present invention.
  • the present inventors found that the impurity concentration and its distribution (or differences in the concentration) near the interface between the amorphous (including fine crystalline state) silicon thin film and the underlying film (e.g. silicon dioxide film) is controlled so as to make the state for generating crystal nucleuses almost uniform and to make the crystal state (crystal grain size and crystal orientation) of polycrystalline film after heat treatment stable (or uniform).
  • the amorphous (including fine crystalline state) silicon thin film and the underlying film e.g. silicon dioxide film
  • the present inventors found that it is effective to form a layer not containing an impurity near the interface of underlying film (i.e. on the underlying film), near the interface of underlying film (i.e. on the underlying film).
  • the direction of crystal plane of polycrystalline layer after crystallization becomes almost uniform, so that the above-mentioned object can be attained due to stabilization of crystal state.
  • the semiconductor device resulting from the method the present invention comprises a semiconductor substrate, an underlying film formed thereon and a polycrystalline silicon thin film doped with an impurity selected from group III and V elements and formed on the underlying film, crystal grains of said silicon thin film having mainly a columnar structure grown from an interface of the underlying film to a surface of the silicon thin film, and a crystal orientation on film surfaces of individual crystal grains being in an almost uniform direction.
  • the semiconductor substrate there can be used conventional ones such as a silicon single crystal substrate, a so-called SOI (silicon-on-insulator) substrate, a wafer obtained by epitaxial growth, and the like.
  • the underlying film there can be used films of SiO 2 , SiN, N 2 O (oxynitride), Ta 2 O 5 , ferroelectric metals of PZT (complex of oxides of Pb, Zr and Ti), or a laminate structure thereof.
  • the impurity there can be used an element selected from group III and V elements such as P (phosphorus), B (boron), As (arsenic), etc. singly or as a mixture thereof.
  • the expression "in an almost uniform direction” means that crystal graphic direction of polycrystalline grains is the same in 60% or more, preferably 80% or more, more preferably 90% or more.
  • a gate oxide film is used as the underlying film and a gate electrode is made from a polycrystalline silicon thin film.
  • the semiconductor device comprises a silicon single crystal substrate, a gate oxide film and a gate electrode formed on the gate oxide film, said gate electrode being made from a silicon thin film doped with an impurity selected from group III and V elements, said silicon thin film being deposited on the gate oxide film, crystal gains of said silicon thin film having mainly a columnar structure grown from an interface of the gate oxide film to a surface of the silicon thin film, and a crystal orientation of film surfaces of individual crystal grains being in an almost uniform direction.
  • Such a semiconductor device can be produced by forming an underlying film on a semiconductor substrate using a conventional method, and forming a silicon thin film on the underlying film by depositing a silicon film having no impurity from a raw material gas such as a SiH 4 gas or a Si 2 H 6 gas to a thickness of 1 nm or more, followed by deposition of the silicon film doped with an impurity selected from group III and V elements, followed by heat treatment at 550°C to 1000°C when the deposited silicon film is an amorphous silicon film to give a polycrystalline silicon thin film.
  • a raw material gas such as a SiH 4 gas or a Si 2 H 6 gas
  • the deposition of silicon thin film is carried out at 500°C to 700°C in the case of polycrystalline silicon thin film, or at 500°C to 600°C in the case of amorphous silicon thin film.
  • the average concentration of impurity in the thin film is about 10 18 - 10 21 number of atom per cm 3
  • the silicon concentration in the thin film is about 5 ⁇ 10 22 number of atom per cm 3 .
  • the amorphous silicon thin film is formed, for example, on a thermal oxide film of silicon (as an underlying film) in about 100 nm thick. A part of amorphous state is found to be crystallized.
  • the crystal grains grown in the shape of ellipsoid are silicon single crystals and the (311) plane of silicon crystal is grown to the top surface of the thin film. This is confirmed by an electron diffraction method.
  • the crystal grains grown in the shape of asteroid are polycrystalline silicon and each hand portion of the asteroid shows a sing crystal state having the (111) crystal plane. This is also confirmed by the electron diffraction method.
  • the presence of such thin film in the semi-conductor device is not preferable. It is desirable that the crystal orientation is almost in a uniform direction. Further, internal stress state in the thin film changes depending on orientation of crystal plane.
  • the internal stress value is the highest when the (111) crystal plane grows and decreases with an increase of the crystal plane indices (the direction from the (111) plane to the (211) plane and (311) plane). Measured value of internal stress is 1200 MPa when the crystal plane index is at the (111) plane, 1000 MPa at the (211) plane, and 800 MPa at the (311) plane. This is because in the silicon crystals since the (111) crystal plane has the highest atomic density at the highest denseness plane, the shrinkage of the thin film becomes larger relatively compared with the case of growing other crystal plane.
  • the above-mentioned internal stress value in the thin film is in the case when a simple crystal plane grows.
  • an intermediate value will be taken depending on occupying rates of crystal plane directions of individual crystal grains.
  • the (111) crystal plane which is to take a high internal stress value grows, it is possible to prevent the generation of failure caused by the internal stress of whole of the semiconductor device by changing a semiconductor device structure or a combination of materials used.
  • the stress value to be generated is known, it is possible to avoid the case of impossible to use.
  • the important thing is to establish the homogenuity of the thin film (including variation of stress value) by avoiding the admixed state of crystal grains having different grown crystal planes.
  • the crystals grow as follows.
  • the crystal growth of the silicon thin film can be controlled by positively controlling the P concentration near the interface of underlying layer.
  • this thin film deposition method is very important from the viewpoint of controlling crystal planes of polycrystalline thin film.
  • the semiconductor device using a silicon thin film doped with an impurity of group III or V elements is characterized in that the semiconductor device is produced by controlling the impurity concentration near the interface between the underlying film and the silicon thin film to remarkably low (preferably zero or almost zero) compared with the average impurity concentration in the thin film, and as a result, the crystal plane direction in the polycrystalline silicon thin film after crystallization is in an almost uniform direction.
  • the chemical vapor deposition apparatus suitable for producing such a silicon thin film according to the present invention comprises
  • This Example shows the case of not introducing an impurity near the interface of underlying film as a method of controlling the impurity concentration and distribution thereof near the interface of underlying film.
  • FIG. 1 is a cross-sectional view immediately after the deposition of thin film (after patterning).
  • Fig. 2 is a cross-sectional view after formation of a polycrystalline film and formation of an insulating film 6.
  • MOS metal-oxide-semiconductor
  • numeral 1 denotes a silicon substrate
  • numeral 2 denotes a silicon oxide film
  • numeral 3 denotes a non-doped amorphous silicon layer
  • numeral 4 denotes a P-doped amorphous silicon layer
  • numeral 5 denotes a P-doped polycrystalline silicon film
  • numeral 30 denotes an interface of underlying film.
  • Figs. 3 to 6 are transmission electron microscope photographs showing crystal growth when an amorphous silicon thin film in about 500 nm thick is doped with an impurity such as P (phosphorus) in an average concentration of c.a. 4 ⁇ 10 20 /cm 3 at near the interface of the underlying film, followed by heat treatment for polycrystallization.
  • Figs. 3 to 6 are transmission electron microscope photographs showing crystal growth when an amorphous silicon thin film in about 500 nm thick is doped with an impurity such as P (phosphorus) in an average concentration of c.a. 4 ⁇ 10 20 /c
  • FIG. 3 and 5 are cross-sectional views of the thin film, and Figs. 4 and 6 are surface views of the thin film. Further, Figs. 5 and 6 show the case of forming a non-doped layer.
  • Fig. 7 is a flow chart showing a process for producing a gate electrode film.
  • step (i) deposition of a P-doped silicon thin film begins.
  • a raw material gas e.g. SiH 4 gas or Si 2 H 6 gas
  • a P doping gas e.g. PH 3 gas
  • the deposition of P-doped amorphous silicon film 4 is continued to a predetermined thickness (v).
  • the total thickness and average P concentration of the thin film are made equal to the case of not positively controlling the P concentration near the interface of underlying film.
  • the amorphous silicon thin film shown in Fig. 1 is formed (vi).
  • P-doped polycrystalline silicon film 5 is formed by crystallization.
  • the thus polycrystallized film is obtained by initially growing individual crystal grains from near the interface of underlying film and further growing columnar structure to the thin film surface.
  • Figs. 3 and 5 observed from the cross-sectional direction.
  • the crystal nucleuses of individual crystal grains are generated near the interface of underlying film.
  • the plane shape of crystal grains is divided into two kinds as shown in Fig. 4 when the non-doped layer is not formed. That is, there are crystal grains grown in the asteroid shape and crystal grains grown in the elliptic shape in admixture.
  • crystal grains having the asteroid shape are not admitted and only crystal grains having the elliptic shape are admitted.
  • the elliptic crystals have the (311) crystal plane grown to the thin film surface. This is confirmed by the measured results by electron diffractometry.
  • the thickness of the layer not doped with the impurity is as small as possible so as to make the crystal growth mode uniform and the amount of impurity for doping in the upper layer of the thin film is a sufficient amount for controlling the electric resistance as a whole to a predetermined value.
  • the thickness of 10 nm or less is sufficient to show the above-mentioned effect.
  • the thickness of the layer not containing the impurity is preferably 1 to 10 nm.
  • the predetermined time for depositing the amorphous film means a time necessary for depositing the film having the film thickness in the above-mentioned range.
  • the crystal growth can be controlled by controlling the P concentration at the beginning of the film deposition.
  • the (311) crystal plane grows predominantly by making a time lag of introduction of P, while the (211) crystal plane grows predominantly when P is introduced positively.
  • the thin film having the above-mentioned structure can be formed without divided two steps.
  • the flow of a dopant gas can be started after a predetermined time from the beginning of flow of a raw material gas for forming the silicon thin film.
  • the impurity used as a dopant is not limited to P, and B (boron) or As (arsenic) can also be used. Therefore, the dopant gas, the doped amorphous silicon film and the polycrystalline silicon thin film can include B or As in place of P. This can also be applied to the Examples mentioned below.
  • the crystallization is conducted after patterning of amorphous silicon film (after the state shown by Fig. 1), but not limited thereto and possible before the patterning. Further, as the impurity, B or As can be used as a dopant in place of P. This can also be applied to the Examples mentioned below.
  • the process of this Example is not limited to the production of the gate electrode of the MOS transistor structure, and can be applied to the production of an emitter electrode, a base electrode and a collector electrode of bipolar transistors, or a gate electrode, a floating electrode, and a control electrode of flash memory structure.
  • This Example is explained referring to Figs. 7, 8 and 9.
  • the present invention is applied to the formation of polycrystalline silicon thin film forming a semiconductor device such as transistors and diodes.
  • Fig. 7 is a flow chart showing the steps for forming the polycrystalline silicon thin film.
  • Fig. 8 is a cross-sectional view showing the state immediately after the deposition of the thin film
  • Fig. 9 is a cross-sectional view of the transistor formed in the polycrystalline silicon thin film, wherein numeral 8 denotes an underlying film, numeral 9 denotes an emitter electrode, numeral 10 denotes a base electrode, numeral 11 is a collector electrode, and numeral 12 is a substrate.
  • numeral 8 denotes an underlying film
  • numeral 9 denotes an emitter electrode
  • numeral 10 denotes a base electrode
  • numeral 11 is a collector electrode
  • numeral 12 is a substrate.
  • the step of introduction of impurity for forming the transistor is omitted, since it has no direct relation to the essence of this Example.
  • an underlying film 8 made from a different material (e.g. SiN) from silicon is formed on a silicon substrate 1.
  • a P-doped silicon thin film is formed (i).
  • the raw material gas e.g. SiH 4 gas or Si 2 H 6 gas
  • a non-doped amorphous silicon layer 3 having the predetermined thickness is formed (iii).
  • an impurity of P as a dopant gas is introduced (iv).
  • the deposition of P-doped amorphous silicon film 4 is continued to obtain the predetermined thickness (v).
  • the thickness of the whole thin film and the average P concentration therein are made equal to the case of not positively controlling the P concentration near the interface of underlying film.
  • Fig. 8 is a cross-sectional view of the thus produced thin film (vi).
  • the base electrode 10, the emitter electrode 9, the collector electrode 11, etc. are formed. These electrodes are not always be required to be formed nearby, and the order of the positions of them can be optional. Further, the transistor formed in the polycrystalline silicon thin film is not always limited to the bipolar transistor, and it can be a diode, or other type of transistor, and the like semiconductor device.
  • the non-doped layer is present near the interface of underlying film under the P-doped amorphous silicon thin film, there can be obtained a polycrystalline layer having the orientation predominantly (90% or more) in the direction of the (311) crystal plane or (211) crystal plane. Further, since the P-doped silicon thin film stable in internal stress can be obtained, properties of the semiconductor device (e.g. transistor) formed in individual crystal grains are low in variation, and thus remarkably stabilized.
  • the semiconductor device e.g. transistor
  • Fig. 10 is a cross-sectional view of a gate electrode in a MOS transistor obtained from the polycrystalline silicon thin film deposited according to the present invention.
  • a P-doped silicon thin film is deposited using a SiH 4 gas on a silicon oxide film 2 formed on a silicon substrate 1 (i).
  • SiH 4 gas raw material gas
  • a non-doped amorphous silicon layer 3 having a predetermined thickness is formed.
  • the film having an orientation in the (311) crystal plane direction is formed (iii).
  • a dopant P gas is introduced (iv).
  • a P-doped amorphous silicon film 4 is deposited continuously to obtain a predetermined thickness (v).
  • the thickness of whole thin film and P concentration therein are made equal to the case of not positively controlling the P concentration near the interface of underlying film (vi).
  • the heat treatment for crystallization is carried out to form the P-doped polycrystalline silicon film 5.
  • the polycrystalline layer having the structure shown in Fig. 10.
  • Fig. 11 is a cross-sectional view of a flash memory, wherein numeral 27 denotes a floating electrode, and numeral 28 denotes a polycrystalline silicon thermal oxidation film.
  • the flash memory comprises a silicon substrate 1, a silicon oxide film 2 (a ultrathin oxidized film) formed thereon, a P-doped polycrystalline silicon film 5 formed on the silicon oxide film, a polycrystalline silicon thermal oxidation film 28 formed by thermal oxidation of the surface of the polycrystalline silicon thin film, and an electroconductive thin film 27 which is to become a floating electrode formed on the polycrystalline silicon thermal oxidation film 28.
  • the P-doped polycrystalline silicon film 5 can be produced either by producing the non-doped layer near the interface of underlying oxide film as described in Example 1.
  • the resulting P-doped polycrystalline silicon film has an orientation in an almost uniform direction as explained previously.
  • the thickness of the thermal oxidation film grown on individual grains becomes uniform. This is a result of losing an influence of the anisotropy wherein the growth speed of oxidation film is different in crystal plane directions, in the case of thermal oxidation of silicon crystals. Thus, it is possible to obtain the uniform film thickness.
  • thermal oxidation film 28 is formed between the P-doped polycrystalline silicon film 5 and the floating electrode 27, but in order to enhance a dielectric constant, it is possible to form a silicon nitride film or a laminate of a silicon nitride film and a silicon oxide film between the thermal oxidation film 28 and the floating electrode 27. It is also possible to use B or As as a dopant in place of P.
  • the film thickness of the thermal oxidation film can be formed uniformly locally (in the unit of each crystal grain) between the P-doped polycrystalline silicon film 5 and the floating electrode 28, it is possible to control the variation of pressure resistance caused by variation in the oxidation film thickness and to design the thickness of the oxidation film as thin as possible.
  • FIG. 12 is a schematic view of a chemical vapor deposition (CVD) apparatus, wherein numeral 20 denotes a reaction chamber for depositing the thin film, numeral 21 denotes a gas introducing unit, numeral 22 denotes a gas flow control valve, numeral 23 denotes a gas bomb for depositing a silicon thin film, numeral 24 denotes a gas bomb for introducing an impurity element, numeral 25 denotes a film deposition control unit in the reaction chamber, numeral 26 denotes a gas exhaust unit, numeral 31 is a wafer and numeral 32 is a board.
  • an upright type CVD apparatus is shown (a heater is not shown in the drawing), but it is possible to use a lateral type CVD apparatus or a sheet treating type.
  • the film deposition control unit 25 is to control the temperature in the reaction chamber, and to control transport of a substrate on which the thin film is to be deposited.
  • the gas bomb 23 is used for storing the raw material gas (e.g. SiH 4 gas or Si 2 H 6 gas) for depositing the silicon thin film.
  • the gas bomb 24 is used for storing the impurity gas as a dopant such as P, B, As, etc.
  • the gas introducing unit 21 controls the timing of introducing each gas into the reaction chamber 20 and the timing of opening or closing the gas flow control valve 22 for depositing the P-doped silicon thin film according to the process shown in Fig. 7.
  • each one path for introducing the raw material gas and the impurity gas is shown, but it is possible to use a plurality of pipes for introducing these gases into the reaction chamber 20. In either case, the gas introduction paths and gas introduction timing should be controlled by the gas introducing unit 21.
  • the impurity-doped silicon thin film can be either an amorphous silicon layer or a polycrystalline silicon layer.
  • crystal orientation of (311) plane, (211) plane or (111) plane is illustrated but not limited thereto.
  • the crystal plane can also include the (100) plane, (110) plane, and the like.
  • the polycrystalline silicon thin film and the semiconductor device using the silicon thin crystal can be controlled to have an almost uniform crystal plane direction, thus the homogeneous polycrystalline silicon thin film having a stabilized internal stress value can be produced stably in a high yield.

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Recrystallisation Techniques (AREA)
  • Electrodes Of Semiconductors (AREA)
  • Non-Volatile Memory (AREA)
  • Insulated Gate Type Field-Effect Transistor (AREA)
  • Thin Film Transistor (AREA)

Claims (9)

  1. Verfahren zur Herstellung einer Dünnschichtelektrode (5) aus polykristallinem Silizium, das mit einer Verunreinigung, ausgewählt aus Elementen der Gruppen III oder V dotiert ist, auf einer darunter liegenden Schicht (2) eines Substrats (1) eines Halbleiterbauteils, wobei eine reine amorphe Siliziumschicht (3) auf der darunter liegenden Schicht (2) abgeschieden wird und die Konzentration und die Verteilung der Verunreinigung in der Nähe der Grenzfläche (30) zwischen der reinen amorphen Siliziumschicht (3) und der darunter liegenden Schicht (2) gesteuert wird durch
    Abscheiden der reinen amorphen Siliziumschicht (3) aus reinem SH4-Gas und/oder S2H6-Gas auf der darunter liegenden Schicht (2) bis zu einer Dicke von 1 - 10 nm,
    Abscheiden einer amorphen, in-situ dotierten Siliziumschicht (4) aus einer Gasmischung aus SH4-Gas und/oder S2H6-Gas auf der amorphen reinen Siliziumschicht, wobei ein Gas das Dotierungselement (3) enthält, und wobei die resultierende amorphe Schicht (4) eine Dotierungselementkonzentration aufweist, die ausreichend ist, um für einen geringen Widerstand der polykristallinen Dünnschichtelektrode (5) zu sorgen, und
    Wärmebehandeln zur Kristallisation der abgeschiedenen amorphen Schichten (3, 4), so dass die Siliziumkörner der polykristallinen Siliziumdünnschicht (5) von der Grenzfläche (30) zur Oberfläche der Dünnschichtelektrode (5) in einer im wesentlichen säulenförmigen Struktur wachsen mit einer gleichmäßigen Orientierung von mindestens 60 % der Kristalle der resultierenden Dünnschicht (5), die in der gleichen Richtung orientiert sind.
  2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, dass die Kristalle der polykristallinen Siliziumschicht (5) wachsen, wobei die (211)- oder die (311)-Kristallebene in der Oberfläche der Dünnschicht (5) orientiert ist.
  3. Verfahren nach einem der Ansprüche 1 oder 2, dadurch gekennzeichnet, dass das Abscheiden der amorphen Schichten (3, 4) aus der Gasphase bei einer Temperatur von 500 bis 600 °C durchgeführt wird.
  4. Verfahren nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass die Polykristallisations-Wärmebehandelung der amorphen Schichten (3, 4) bei einer Temperatur von 550 bis 1000 °C durchgeführt wird.
  5. Verfahren nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass das Aufbringen einer Gate-Elektrode nach der Bildung der zweiten Siliziumschicht (4) und vor der Wärmebehandlung durchgeführt wird.
  6. Verfahren nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass das Dotierungselement Phosphor, Bor, Arsen oder eine Mischung davon ist.
  7. Verfahren nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass die zweite amorphe Siliziumschicht (4) nach einer vorbestimmten Zeit nach dem Zuführen von reinem Si-Gas zur Bildung der ersten amorphen Siliziumschicht (3) gebildet wird.
  8. Verfahren nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass die zweite amorphe Siliziumschicht aus einem Gas mit SiH2- oder Si2H6-Material abgeschieden wird, das PH3 enthält.
  9. Verfahren nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, dass das Halbleiterbauteil ein Metalloxidhalbleiter(metal-oxide-semidconductor, MOS)-Transistor ist.
EP95114554A 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysilicium-Schicht und Verfahren zur Herstellung Expired - Lifetime EP0707344B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP02001183A EP1209726A3 (de) 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysiliziumschicht und Vefahren zur Herstellung

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP248310/94 1994-09-19
JP24831094A JP3599290B2 (ja) 1994-09-19 1994-09-19 半導体装置
JP24831094 1994-09-19

Related Child Applications (1)

Application Number Title Priority Date Filing Date
EP02001183A Division EP1209726A3 (de) 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysiliziumschicht und Vefahren zur Herstellung

Publications (3)

Publication Number Publication Date
EP0707344A2 EP0707344A2 (de) 1996-04-17
EP0707344A3 EP0707344A3 (de) 1996-08-28
EP0707344B1 true EP0707344B1 (de) 2002-08-21

Family

ID=17176178

Family Applications (2)

Application Number Title Priority Date Filing Date
EP02001183A Withdrawn EP1209726A3 (de) 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysiliziumschicht und Vefahren zur Herstellung
EP95114554A Expired - Lifetime EP0707344B1 (de) 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysilicium-Schicht und Verfahren zur Herstellung

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP02001183A Withdrawn EP1209726A3 (de) 1994-09-19 1995-09-15 Halbleiteranordnung mit einer dünnen Polysiliziumschicht und Vefahren zur Herstellung

Country Status (7)

Country Link
US (5) US5670793A (de)
EP (2) EP1209726A3 (de)
JP (1) JP3599290B2 (de)
KR (3) KR100270192B1 (de)
CN (1) CN1054235C (de)
DE (1) DE69527827T2 (de)
TW (2) TW541684B (de)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3599290B2 (ja) * 1994-09-19 2004-12-08 株式会社ルネサステクノロジ 半導体装置
JPH11145056A (ja) * 1997-11-07 1999-05-28 Sony Corp 半導体材料
US6429101B1 (en) * 1999-01-29 2002-08-06 International Business Machines Corporation Method of forming thermally stable polycrystal to single crystal electrical contact structure
US6235586B1 (en) * 1999-07-13 2001-05-22 Advanced Micro Devices, Inc. Thin floating gate and conductive select gate in situ doped amorphous silicon material for NAND type flash memory device applications
JP4389359B2 (ja) * 2000-06-23 2009-12-24 日本電気株式会社 薄膜トランジスタ及びその製造方法
US6621114B1 (en) * 2002-05-20 2003-09-16 Advanced Micro Devices, Inc. MOS transistors with high-k dielectric gate insulator for reducing remote scattering
JP2004133329A (ja) * 2002-10-15 2004-04-30 Hitachi Ltd 非線形光学薄膜及びそれを用いた非線形光学素子並びにそれを用いた光スイッチ
US7180160B2 (en) 2004-07-30 2007-02-20 Infineon Technologies Ag MRAM storage device
US7410910B2 (en) 2005-08-31 2008-08-12 Micron Technology, Inc. Lanthanum aluminum oxynitride dielectric films
WO2007046290A1 (en) * 2005-10-18 2007-04-26 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and manufacturing method thereof
US8278739B2 (en) * 2006-03-20 2012-10-02 Semiconductor Energy Laboratory Co., Ltd. Crystalline semiconductor film, semiconductor device, and method for manufacturing thereof
US7662703B2 (en) * 2006-08-31 2010-02-16 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing crystalline semiconductor film and semiconductor device
US7935584B2 (en) * 2006-08-31 2011-05-03 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing crystalline semiconductor device
US7972943B2 (en) * 2007-03-02 2011-07-05 Semiconductor Energy Laboratory Co., Ltd. Manufacturing method of semiconductor device
DE102011002236A1 (de) * 2011-04-21 2012-10-25 Dritte Patentportfolio Beteiligungsgesellschaft Mbh & Co.Kg Verfahren zur Herstellung einer polykristallinen Schicht
CN102154629B (zh) * 2011-05-30 2013-03-13 上海森松化工成套装备有限公司 多晶硅cvd炉混合气进出量调节装置及其调节方法
KR101706747B1 (ko) * 2015-05-08 2017-02-15 주식회사 유진테크 비정질 박막의 형성방법
KR102426015B1 (ko) * 2015-09-24 2022-07-27 삼성디스플레이 주식회사 다결정 규소막 검사 장치 및 검사 방법
CN106876249B (zh) * 2017-02-23 2019-04-26 河南仕佳光子科技股份有限公司 一种二氧化硅厚膜的制备方法
CN108149216A (zh) * 2017-12-07 2018-06-12 上海申和热磁电子有限公司 一种改善低压化学气相淀积多晶硅薄膜质量的方法
EP3599290A3 (de) * 2018-07-24 2020-06-03 Lg Electronics Inc. Chemische dampfabscheideanlage für solarzelle und abscheideverfahren dafür
WO2020055820A1 (en) 2018-09-10 2020-03-19 Boston Scientific Scimed, Inc. Introducer with expandable capabilities
KR102760046B1 (ko) * 2018-12-14 2025-01-24 에스케이하이닉스 주식회사 반도체장치 및 그 제조 방법

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254960A (en) * 1991-04-19 1992-10-21 Samsung Electronics Co Ltd Gate electrode for a mos device and manufacture

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5244500A (en) * 1983-10-05 1993-09-14 Toshiba Kikai Kabushiki Kaisha Process control system of semiconductor vapor phase growth apparatus
CA1239706A (en) * 1984-11-26 1988-07-26 Hisao Hayashi Method of forming a thin semiconductor film
JPS61237420A (ja) * 1985-04-13 1986-10-22 Oki Electric Ind Co Ltd P型アモルフアスシリコン薄膜の製造方法
US5769950A (en) * 1985-07-23 1998-06-23 Canon Kabushiki Kaisha Device for forming deposited film
JPS6254423A (ja) 1985-08-23 1987-03-10 Semiconductor Energy Lab Co Ltd 半導体装置作製方法
JPS6276677A (ja) * 1985-09-30 1987-04-08 Toshiba Corp 半導体装置の製造方法
JPS63236310A (ja) * 1987-03-25 1988-10-03 Nippon Soken Inc 半導体素子及びその製造方法
US5153702A (en) * 1987-06-10 1992-10-06 Hitachi, Ltd. Thin film semiconductor device and method for fabricating the same
US5518937A (en) * 1988-03-11 1996-05-21 Fujitsu Limited Semiconductor device having a region doped to a level exceeding the solubility limit
EP0332101B1 (de) * 1988-03-11 1997-06-04 Fujitsu Limited Halbleiterbauelement mit einem über die Löslichkeitsgrenze dotierten Bereich
EP0598409B1 (de) * 1989-02-14 1998-11-18 Seiko Epson Corporation Verfahren zur Herstellung einer Halbleitervorrichtung
DE69033153T2 (de) * 1989-03-31 1999-11-11 Canon K.K., Tokio/Tokyo Verfahren zur Herstellung einer Halbleiterdünnschicht und damit hergestellte Halbleiterdünnschicht
JP2797200B2 (ja) * 1989-08-10 1998-09-17 日本電信電話株式会社 多結晶シリコン電極およびその製造方法
CA2031254A1 (en) * 1989-12-01 1991-06-02 Kenji Aoki Doping method of barrier region in semiconductor device
JP3070126B2 (ja) 1990-05-09 2000-07-24 大日本インキ化学工業株式会社 架橋ウレタン−尿素樹脂分散体およびその製造法
US5254208A (en) * 1990-07-24 1993-10-19 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing a semiconductor device
US5318919A (en) * 1990-07-31 1994-06-07 Sanyo Electric Co., Ltd. Manufacturing method of thin film transistor
JPH04137724A (ja) 1990-09-28 1992-05-12 Tonen Corp 多結晶シリコン薄膜
JPH04151823A (ja) * 1990-10-15 1992-05-25 Mitsubishi Electric Corp 半導体装置およびその製造方法
JP2875380B2 (ja) * 1990-11-19 1999-03-31 三菱電機株式会社 半導体装置およびその製造方法
JP2875379B2 (ja) * 1990-11-19 1999-03-31 三菱電機株式会社 半導体装置およびその製造方法
JPH04196311A (ja) * 1990-11-28 1992-07-16 Fujitsu Ltd 半導体装置の製造方法
KR970009976B1 (ko) * 1991-08-26 1997-06-19 아메리칸 텔리폰 앤드 텔레그라프 캄파니 증착된 반도체상에 형성된 개선된 유전체
JPH05343316A (ja) * 1991-09-30 1993-12-24 Nec Corp 半導体装置の製造方法
JPH0620990A (ja) * 1992-07-03 1994-01-28 Nec Corp 半導体装置の製造方法
JPH0621460A (ja) * 1992-07-03 1994-01-28 Seiko Epson Corp 半導体装置及び半導体装置の製造方法
KR940003085A (ko) * 1992-07-15 1994-02-19 김광호 고압 및 저압용 mos 트랜지스터 반도체 장치 제조방법 및 그 장치
JP3185396B2 (ja) * 1992-09-11 2001-07-09 富士電機株式会社 半導体装置の製造方法
US5444302A (en) * 1992-12-25 1995-08-22 Hitachi, Ltd. Semiconductor device including multi-layer conductive thin film of polycrystalline material
US5563093A (en) * 1993-01-28 1996-10-08 Kawasaki Steel Corporation Method of manufacturing fet semiconductor devices with polysilicon gate having large grain sizes
KR960002086B1 (ko) * 1993-04-16 1996-02-10 엘지전자주식회사 박막 트랜지스터의 제조방법
JP3322440B2 (ja) * 1993-06-24 2002-09-09 三洋電機株式会社 薄膜多結晶シリコンの製造方法
JP2771472B2 (ja) * 1994-05-16 1998-07-02 松下電器産業株式会社 半導体装置の製造方法
US5438019A (en) * 1994-07-11 1995-08-01 Micron Semiconductor, Inc. Large area thin film growing method
JP3599290B2 (ja) * 1994-09-19 2004-12-08 株式会社ルネサステクノロジ 半導体装置
US5753555A (en) * 1995-11-22 1998-05-19 Nec Corporation Method for forming semiconductor device

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254960A (en) * 1991-04-19 1992-10-21 Samsung Electronics Co Ltd Gate electrode for a mos device and manufacture

Also Published As

Publication number Publication date
EP0707344A3 (de) 1996-08-28
TW475252B (en) 2002-02-01
KR960012313A (ko) 1996-04-20
KR100396400B1 (ko) 2003-09-03
US5670793A (en) 1997-09-23
EP0707344A2 (de) 1996-04-17
JPH0888173A (ja) 1996-04-02
KR100270192B1 (ko) 2000-12-01
US6080611A (en) 2000-06-27
EP1209726A3 (de) 2002-10-09
KR100397086B1 (ko) 2003-09-06
DE69527827T2 (de) 2003-04-03
US6559037B2 (en) 2003-05-06
JP3599290B2 (ja) 2004-12-08
CN1128898A (zh) 1996-08-14
EP1209726A2 (de) 2002-05-29
US6204155B1 (en) 2001-03-20
CN1054235C (zh) 2000-07-05
TW541684B (en) 2003-07-11
US20020013038A1 (en) 2002-01-31
DE69527827D1 (de) 2002-09-26
US6187100B1 (en) 2001-02-13

Similar Documents

Publication Publication Date Title
EP0707344B1 (de) Halbleiteranordnung mit einer dünnen Polysilicium-Schicht und Verfahren zur Herstellung
US6391749B1 (en) Selective epitaxial growth method in semiconductor device
EP0521644B1 (de) Verfahren zur Herstellung eines polykristallinen Siliziumfilmes
JP2689935B2 (ja) 半導体薄膜形成方法
KR100299784B1 (ko) 요철상폴리실리콘층의형성방법및이방법의실시에사용되는기판처리장치와반도체메모리디바이스
JP2002203809A (ja) 半導体装置及びその製造方法
US7553742B2 (en) Method(s) of forming a thin layer
US8102052B2 (en) Process for the simultaneous deposition of crystalline and amorphous layers with doping
JPH0563439B2 (de)
US5464795A (en) Method of forming polycrystalline silicon thin films for semiconductor devices
JP3006396B2 (ja) 半導体薄膜の形成方法
JP2004281591A (ja) 半導体エピタキシャルウエハとその製法,半導体装置及びその製法
JP2707985B2 (ja) 半導体装置の製造方法
GB2326648A (en) Growth of polycrystalline silicon film by raising temperature during deposition
JPH097909A (ja) 半導体装置の製造方法
JP3064363B2 (ja) Si薄膜の形成方法
KR100196596B1 (ko) 반도체 박막의 형성 방법
JPH0547702A (ja) 不純物ドープト半導体膜製造方法
CN114267628A (zh) 超薄绝缘体上硅(soi)衬底基片及其制备方法
GB2335929A (en) Deposition using a movable screening means

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB IT

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB IT

17P Request for examination filed

Effective date: 19960724

17Q First examination report despatched

Effective date: 19980319

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB IT

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 69527827

Country of ref document: DE

Date of ref document: 20020926

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20030522

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20120912

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20120926

Year of fee payment: 18

Ref country code: DE

Payment date: 20120912

Year of fee payment: 18

Ref country code: IT

Payment date: 20120914

Year of fee payment: 18

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20130915

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 69527827

Country of ref document: DE

Effective date: 20140401

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20140530

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20130915

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140401

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20130915

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20130930